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| created at |
2024-09-23 16:23:50 UTC |
| updated at |
2024-09-23 18:22:39 UTC |
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Terms for rare diseases as defined in ORDO.
The entries were initially sourced from the ORDO version 2024-07-03 as stored in BioPortal.
Namespace: http://www.orpha.net/ORDO/
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20,514 entries
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There is 0 pattern entry.
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CRAO
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Orphanet_648684 |
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Noonan syndrome
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Orphanet_648 |
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Rare scleritis
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Orphanet_648559 |
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Ferroportin disease
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Orphanet_648562 |
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Non-HFE-related hemochromatosis
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Orphanet_648569 |
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Digenic hemochromatosis
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Orphanet_648581 |
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Infectious scleritis
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Orphanet_648665 |
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Idiopathic scleritis
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Orphanet_648675 |
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Immune-mediated scleritis
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Orphanet_648681 |
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Idiopathic catatonia
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Orphanet_648919 |
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Isolated catatonia
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Orphanet_648919 |
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Central retinal artery occlusion
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Orphanet_648684 |
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Non-syndromic bridging bronchus
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Orphanet_648992 |
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Idiopathic catatonic syndrome
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Orphanet_648919 |
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Isolated catatonic syndrome
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Orphanet_648919 |
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